Last synced on 19 July 2024 at 11:05 pm

DISPO ETCH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984380
510(k) Type
Traditional
Applicant
KIS PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2001
Days to Decision
972 days
Submission Type
Summary

DISPO ETCH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984380
510(k) Type
Traditional
Applicant
KIS PRODUCTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2001
Days to Decision
972 days
Submission Type
Summary